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Diphenylpyraline hydrochloride

Synonyms: 盐酸双苯比拉林, 4-Diphenylmethoxy-1-methylpiperidine hydrochloride
货号 T0059Cas号 132-18-3 一键复制产品信息纯度: 98.72%
Rating icon 很棒

Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) 是一种组胺 H1 受体的拮抗剂,抑制多巴胺的吸收。它是可口服的抗组胺试剂,具有抗胆碱和抗过敏作用,可用于缓解过敏性疾病,如鼻炎、花粉热和瘙痒性皮肤疾病等。

Diphenylpyraline hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 98.72%

货号 T0059Cas号 132-18-3

别名 盐酸双苯比拉林, 4-Diphenylmethoxy-1-methylpiperidine hydrochloride

Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) 是一种组胺 H1 受体的拮抗剂,抑制多巴胺的吸收。它是可口服的抗组胺试剂,具有抗胆碱和抗过敏作用,可用于缓解过敏性疾病,如鼻炎、花粉热和瘙痒性皮肤疾病等。

Diphenylpyraline hydrochloride
其他形式的 “Diphenylpyraline hydrochloride”:
规格价格库存数量
500 mg
¥ 123
现货
1 mL x 10 mM (in DMSO)
¥ 250
现货
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选择批次:
纯度: 98.72%
颜色: 白色
性状: Solid
资源下载: COA HNMR HPLC LCMS产品操作手册

产品介绍


Diphenylpyraline hydrochloride AI Summary
Diphenylpyraline hydrochloride exhibits a multifaceted bioactivity profile. It demonstrates antimicrobial activity against Mycobacterium tuberculosis H37Rv with an inhibition rate of 5.0% at 6.25 µg/mL and an MIC of 64.0 µg/mL. Additionally, it exhibits cytotoxicity against HEK293 cells with an LC50 value of 107.59 µg/mL. The compound shows inhibition of several key biological targets: 1. Inhibition of IMPase with a potency of 2238.7 nM. 2. Moderate inhibition of the ERK signaling pathway with a potency of 39810.7 nM. 3. Inhibition of AmpC Beta-Lactamase and Histone Lysine Methyltransferase G9a, both with a potency of 89125.1 nM. 4. Inhibition of the malarial parasite plastid with a potency of 18526.0 nM. 5. Inhibition of viral entry mechanisms for Lassa Virus, Marburg Virus, and Ebola Virus with potencies ranging from 12589.3 nM to 3548.1 nM. 6. Activity in a cell-based assay for B-Galactocerebrosidase with a potency of 707.9 nM. Furthermore, Diphenylpyraline hydrochloride significantly inhibits OATP1B3 and OATP1B1 transporters with 87.39% and 68.46% inhibition at 10 µM, respectively. It also demonstrates antiviral activity against SARS-CoV-2 by inhibiting cytotoxicity in Caco-2 cells and VERO-6 cells at 10 µM, with inhibition rates of 13.81% and -0.01% respectively, and by inhibiting the SARS-CoV-2 3CL-Pro protease by 23.7% at 20 µM. Diphenylpyraline hydrochloride, however, shows lower activity against SARS-CoV-2-induced cytotoxicity in Vero E6 cells compared to the arbidol control, with an inhibition index of 0.8198. Overall, Diphenylpyraline hydrochloride is a versatile bioactive compound with potential applications in antimicrobial and antiviral therapies, as well as in modulating various cellular pathways..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) is used in the treatment of Parkinsonism.It is a first-generation antihistamine with anticholinergic effects, functions as a dopamine reuptake inhibitor.
别名
盐酸双苯比拉林, 4-Diphenylmethoxy-1-methylpiperidine hydrochloride
化学信息
分子量317.85
分子式C19H23NO·HCl
CAS No.132-18-3
SmilesCl.CN1CCC(CC1)OC(c1ccccc1)c1ccccc1
密度no data available
储存&溶解度
存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

实际储存温度请以COA为准

溶解度信息
DMSO: 55 mg/mL (173.04 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.29 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.1461 mL15.7307 mL31.4614 mL157.3069 mL
5 mM0.6292 mL3.1461 mL6.2923 mL31.4614 mL
10 mM0.3146 mL1.5731 mL3.1461 mL15.7307 mL
20 mM0.1573 mL0.7865 mL1.5731 mL7.8653 mL
50 mM0.0629 mL0.3146 mL0.6292 mL3.1461 mL
100 mM0.0315 mL0.1573 mL0.3146 mL1.5731 mL
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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